2,319 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Specialist, Clinical Research Monitoring, Manager, Clinical Research Monitoring, Community IBC Member (Augusta), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Perform field monitoring of clinical trials to ensure data consistency and compliance with GCP and regulatory requirements. Provide oversight of trial activities, mentor junior staff, and contribute to the development of clinical protocols and informed consent forms.
Lead field monitoring and data collection for complex clinical trials while ensuring compliance with GCP and regulatory requirements. Provide strategic direction, mentor junior staff, and oversee trial conduct including metrics and protocol deviations.
The member reviews research protocols and monitors regulatory compliance to ensure the protection of participants, animals, and biosafety standards. They provide recommendations for the approval or termination of studies and assess risks associated with hazardous biological work.
Coordinate and execute clinical trial monitoring activities, including site visits and study status reporting. Maintain strong relationships with stakeholders and ensure patient safety through strict compliance with protocols and regulatory requirements.
Serve as a senior strategic leader driving business growth and strengthening sponsor relationships within medical imaging and cardiac safety services. Provide expert guidance on study strategy, operational delivery, and scientific innovation for global clinical development programs.
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The Sr. CRA is responsible for monitoring clinical trials to ensure adherence to protocols, regulations, and SOPs while acting as the primary liaison to clinical sites. Key duties include conducting site visits, verifying source data, and contributing to the development of study plans and regulatory reports.
Design and specify study data tabulation and analysis models for clinical trials in accordance with industry standards. Develop SAS programming codes to generate accurate statistical output reports and provide technical guidance to junior programmers.
The role involves managing cross-functional projects and administering the contracting process for Lupus Therapeutics. Key duties include preparing agreements, tracking budgets, and coordinating with biopharmaceutical partners and outside counsel.
Facilitate the development and preparation of high-quality proposals for clinical trials by collaborating with cross-functional teams and subject matter experts. Manage timelines, ensure compliance with client requirements, and mentor colleagues in the proposal process.
Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.
The Auditor/Educator Physician reviews medical records for coding accuracy and provides feedback and education to improve documentation. They also create action plans and training materials to address coding problems and documentation gaps.
Review medical records for coding accuracy and provide feedback to coders and providers. Deliver education to improve documentation and coding practices.
The Medical Science Liaison (MSL) is responsible for building partnerships with key opinion leaders and engaging in scientific exchanges with external stakeholders. This includes providing medical support, delivering education, and fostering collaborations in the assigned therapeutic areas.
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for early-stage development clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
The analyst is responsible for delivering high-quality eCOA solution designs by translating pharmaceutical client requirements and study protocols into optimized specifications. They coordinate the design process and collaborate with cross-functional teams to ensure data integrity and efficient project delivery.
Responsible for all aspects of clinical site monitoring, including initiation, routine visits, and close-out of oncology trials. Ensures data integrity, patient safety, and adherence to study protocols and regulatory requirements.
Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.
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Lead the management and coordination of medical projects to ensure compliance and optimal performance throughout the project lifecycle. Perform safety data reviews, manage project financials, and serve as the primary point of contact for clinical project teams.
Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Identify safety trends, resolve complex issues, and support the creation of safety and medical management plans.
The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, alignment, and optimal performance throughout the project lifecycle. This includes reviewing safety data, managing project financials, and serving as the primary point of contact for clinical project teams.
The VP Strategic Advisory Partnerships will position Omega as a partner of choice within the advisory ecosystem and drive measurable revenue through influenced and co-developed sales opportunities. Responsibilities include developing relationships with advisory firms, identifying opportunities for collaboration, and enabling revenue generation through strategic partnerships.
Monitor the collection and analysis of data from third-party suppliers for sponsored clinical trials. Evaluate supplier compliance, track corrective actions, and maintain professional relationships with external stakeholders.
The Attorney 1 will prepare SEC filings and provide counsel on compliance, governance, and capital markets transactions. They will also manage legal entity reorganizations and coordinate sustainability reporting requirements.
The Associate Director of Clinical Affairs is responsible for creating and executing clinical strategies, including the design and support of clinical studies and protocol development. This role involves overseeing CROs and collaborating with cross-functional teams to facilitate trial enrollment and regulatory compliance.
Provide advanced technical expertise to develop process methodology and integrated programming solutions for complex clinical studies. Lead technical teams in creating statistical tables, figures, listings, and analysis datasets while coordinating with internal and external clients.
Lead global and regional clinical programs from start-up to close-out while managing and coaching a team of Study Managers. Drive cross-functional collaboration and maintain relationships with external partners, KOLs, and CROs to ensure high-quality study delivery.
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Provide high-quality medical information services via phone and email, answering technical product questions and handling adverse event reports. Translate medical documents between English and Spanish and ensure all inquiries are logged accurately in compliance with SOPs.
The Senior Medical Director provides strategic and scientific leadership across multiple brands to ensure the accuracy and impact of medical communications. This role involves overseeing medical strategy, mentoring junior staff, and collaborating with multidisciplinary teams to drive business growth.
The Clinical Operations Lead provides oversight of project deliverables, CRAs, and investigator sites to ensure compliance with protocols and GCP guidelines. They act as the primary liaison between the monitoring team and the clinical project team while managing site performance and recruitment strategies.
The MSL will engage in peer-to-peer scientific dialogue with healthcare professionals and KOLs to gather insights and advance medical knowledge. They will serve as a therapeutic expert and liaison between the company and clinical study sites, supporting medical congresses and advisory boards.
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